Canonical Allele Identifier: CA382619327

Gene: SDHD

Linked Data

• MyVariant Identifiers: chr11:g.111965635T>G (hg19) ; chr11:g.112094911T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094911T>G , CM000673.2:g.112094911T>G	GRCh38
NC_000011.9:g.111965635T>G , CM000673.1:g.111965635T>G	GRCh37
NC_000011.8:g.111470845T>G	NCBI36
NG_012337.2:g.13065T>G
NG_012337.3:g.13065T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*160T>G	ENSP00000432946.2:n.*160T>G
ENST00000534010.2:c.314+5900T>G	ENSP00000433202.2:n.314+5900T>G
ENST00000375549.8:c.421T>G MANE Select	ENSP00000364699.3:p.Tyr141Asp
ENST00000528021.6:c.314+5900T>G	ENSP00000432465.1:n.314+5900T>G
ENST00000375549.7:c.421T>G	ENSP00000364699.3:p.Tyr141Asp
ENST00000525291.5:c.304T>G	ENSP00000436669.1:p.Tyr102Asp
ENST00000525987.5:n.319+5900T>G
ENST00000526592.5:c.*119T>G	ENSP00000432005.1:n.*119T>G
ENST00000528021.5:c.314+5900T>G	ENSP00000432465.1:n.314+5900T>G
ENST00000528048.5:c.*18T>G	ENSP00000436217.1:n.*18T>G
ENST00000528182.5:c.*18T>G	ENSP00000435475.1:n.*18T>G
ENST00000530923.5:c.465T>G
ENST00000531744.5:c.314+5900T>G	ENSP00000456957.1:n.314+5900T>G
ENST00000532699.1:c.314+5900T>G	ENSP00000456434.1:n.314+5900T>G
ENST00000534010.1:c.145+5900T>G
NM_001276503.1:c.*18T>G	NP_001263432.1:n.*18T>G
NM_001276504.1:c.304T>G	NP_001263433.1:p.Tyr102Asp
NM_001276506.1:c.*119T>G	NP_001263435.1:n.*119T>G
NM_003002.3:c.421T>G	NP_002993.1:p.Tyr141Asp
NR_077060.1:n.559T>G
NM_003002.4:c.421T>G MANE Select	NP_002993.1:p.Tyr141Asp
NM_001276503.2:c.*18T>G	NP_001263432.1:n.*18T>G
NM_001276504.2:c.304T>G	NP_001263433.1:p.Tyr102Asp
NM_001276506.2:c.*119T>G	NP_001263435.1:n.*119T>G
NR_077060.2:n.510T>G